Clinical trial

High-Dose Cytarabine Plus Deoxycytidine in Treating With Acute Myelogenous…

NCT00002818 · Virginia Commonwealth University, Other · Completed

Key facts

NCT number NCT00002818
Title High-Dose Cytarabine Plus Deoxycytidine in Treating With Acute Myelogenous Leukemia or Other Hematologic Malignancies
Official title Phase I and Clinical Pharmacokinetic De-Escalation Study of 2'-Deoxycitidine Administered as a Continuous Infusion in Conjunction With a Continuous Infusion of High-Dose ARA-C in Patients With Refractory Acute Myelogenous Leukemia
Lead sponsor Virginia Commonwealth University, Other
Collaborators National Cancer Institute (NCI) NIH
Status Completed
Phase Phase 1
Study type Interventional
Conditions Drug/Agent Toxicity by Tissue/Organ, Leukemia, Lymphoma, Multiple Myeloma and Plasma Cell Neoplasm
Intervention type Drug
Interventions cytarabine, deoxycytidine
Enrollment 15
Start date Feb 1, 1995
Primary completion Feb 1, 2001
Completion Feb 1, 2001
First posted Apr 22, 2004
Last update posted Dec 14, 2015
Countries United States

At a glance

  • 1–9 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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